News

Reeling from the deaths of two patients who took Duchenne muscular dystrophy gene therapy Elevidys, Sarepta is launching a ...
Sarepta Therapeutics appears to have right-sized itself after laying off over a third of its staff, announcing a significant ...
On an investor call Friday, analysts grilled the company over its apparent lack of transparency on the matter.
The U.S. Food and Drug Administration is planning to ask Sarepta Therapeutics to voluntarily stop all shipments of its gene ...
In a letter to the patient advocacy group World Duchenne Organization on Monday, Roche (OTCQX:RHHBF) ... Update: 9.28 AM EST: Adds comments from Sarepta. More on Roche, Sarepta, etc.
Sarepta Therapeutics demanded a prominent patient advocacy organization censor a video that contained pointed criticism of the company’s recently approved gene therapy for Duchenne muscular ...
Since the FDA cleared Sarepta Thereapeutics' gene therapy for nearly all people with Duchenne, its stock price has tanked.
Sarepta Forward Looking Statement This press release contains "forward-looking statements." Any statements contained in this press release that are not statements of historical fact may be deemed ...
Sarepta Therapeutics Inc said the U.S. drug regulator could initially approve its gene therapy for a muscle wasting disorder for a smaller patient group after the agency deferred an accelerated ...
Sarepta’s stock jumped more than 30% on Friday following news that the Food and Drug Administration expanded the pool of patients eligible for its Duchenne muscular dystrophy (DMD) drug, Elevidys.